A Study to Assess Benign Joint Hypermobility Syndrome in Children With a History of Wheezing or Asthma

NCT ID: NCT02163096

Last Updated: 2016-01-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

23 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-06-30

Study Completion Date

2015-06-30

Brief Summary

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The purpose of this study is to assess benign joint hypermobility syndrome (BJHS) in children with a history of wheezing or asthma. BJHS is a common syndrome of joint and connective tissue laxity without any other rheumatologic disease. This assessment will be performed by using either method below depending upon if the child has a history of wheezing or severe asthma:

1. Determine the correlation, if there is an increased rate of BJHS in children with a history of wheezing as well as if there is an increased history of wheezing in children with BJHS; or
2. Determine asthma control, lung function and asthma exacerbations (a flare up or acute worsening of symptoms) in children with BJHS compared to children with asthma without BJHS, to assess if it BJHS is associated more with children with severe asthma.

Detailed Description

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Conditions

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Benign Joint Hypermobility Syndrome Wheezing Asthma

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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History of Wheezing, Benign Joint Hypermobility Syndrome

No interventions assigned to this group

Asthma, Benign Joint Hypermobility Syndrome

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* All children ages 6-16 with a history of wheezing or asthma

Exclusion Criteria

* For subjects with a history of Wheezing: History of chronic lung disease or prematurity, chronic aspiration, congenital anomalies of the upper and lower airway, primary ciliary dyskinesia, cystic fibrosis, history of heart failure, immune deficiency, or any inflammatory arthritis.
* For Subjects with a history of Asthma: current acute respiratory exacerbation, history of chronic lung disease of prematurity, chronic aspiration, congenital anomalies of the upper or lower airway, primary ciliary dyskinesia, cystic fibrosis, restrictive lung disease, history of heart failure, immune deficiency, or inflammatory arthritis.
Minimum Eligible Age

6 Years

Maximum Eligible Age

16 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Louisville

OTHER

Sponsor Role lead

Responsible Party

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Ronald L. Morton

Professor of Pediatrics

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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University of Louisville - Sam Swope Kosair Charities Centre

Louisville, Kentucky, United States

Site Status

University of Louisville Allergy and Immunology

Louisville, Kentucky, United States

Site Status

University of Louisville Pediatric Pulmonology

Louisville, Kentucky, United States

Site Status

Countries

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United States

Other Identifiers

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14.0447

Identifier Type: -

Identifier Source: org_study_id

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